Evidence map›Paper›PMID 31265867›Full record

ArticleThe Journal of infection2019

Colistin for the treatment of urinary tract infections caused by extremely drug-resistant Pseudomonas aeruginosa: Dose is critical.

Luisa Sorlí, Sonia Luque, Jian Li, Núria Campillo, Marc Danés, Milagro Montero, Concha Segura, Santiago Grau, Juan Pablo Horcajada

Open access · greenAbstract read
In one paragraph

Article in The Journal of infection, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Global epidemiology of carbapenem-resistantJAC-antimicrobial resistance · 2026
    Review
  2. Article
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  6. Review
  7. Article
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  11. Colistin: Lights and Shadows of an Older Antibiotic.Molecules (Basel, Switzerland) · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Individualized optimization of colistin loading doses.Journal of pharmacokinetics and pharmacodynamics · 2023
    Article
  16. Cells · 2023
    Review
  17. Article
  18. Article
  19. Review
  20. Optimal control for colistin dosage selection.Journal of pharmacokinetics and pharmacodynamics · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Luisa SorlíInfectious Diseases Department, Parc de Salut Mar, Passeig Marítim 25-29, E-08003 Barcelona, Spain; Infectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; CEXS-Universitat Pompeu Fabra (UPF), Barcelona, Spain; Spanish Network for Research in Infectious Diseases (REIPI RD 16/0016/0015), Instituto de Salud Carlos III, Madrid, Spain. Electronic address: lsorli@hospitaldelmar.cat.
Sonia LuqueInfectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; Spanish Network for Research in Infectious Diseases (REIPI RD 16/0016/0015), Instituto de Salud Carlos III, Madrid, Spain; Pharmacy Department, Parc de Salut Mar. Passeig Marítim 25-29, E-08003 Barcelona, Spain; Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Jian LiBiomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, Victoria 3800, Australia.
Núria CampilloInfectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; Pharmacy Department, Parc de Salut Mar. Passeig Marítim 25-29, E-08003 Barcelona, Spain.
Marc DanésCEXS-Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Milagro MonteroInfectious Diseases Department, Parc de Salut Mar, Passeig Marítim 25-29, E-08003 Barcelona, Spain; Infectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; CEXS-Universitat Pompeu Fabra (UPF), Barcelona, Spain; Spanish Network for Research in Infectious Diseases (REIPI RD 16/0016/0015), Instituto de Salud Carlos III, Madrid, Spain; Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Concha SeguraLaboratori de Referència de Catalunya, Carrer de la Selva, 10, E-08820 Prat de Llobregat (El), Barcelona.
Santiago GrauInfectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; Spanish Network for Research in Infectious Diseases (REIPI RD 16/0016/0015), Instituto de Salud Carlos III, Madrid, Spain; Pharmacy Department, Parc de Salut Mar. Passeig Marítim 25-29, E-08003 Barcelona, Spain; Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Juan Pablo HorcajadaInfectious Diseases Department, Parc de Salut Mar, Passeig Marítim 25-29, E-08003 Barcelona, Spain; Infectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain; CEXS-Universitat Pompeu Fabra (UPF), Barcelona, Spain; Spanish Network for Research in Infectious Diseases (REIPI RD 16/0016/0015), Instituto de Salud Carlos III, Madrid, Spain; Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Hospital del Mar Research Institute · ESRed Espanola de Investigacion en Patologia Infecciosa · ESAustralian Regenerative Medicine Institute · AUParc de Salut · ESPompeu Fabra University · ES

Funding

Targeting the Urgent Need for New Antibiotics against Gram-negative ‘Superbugs’R01AI132154 · NIAID · MONASH UNIVERSITY · PI LI, JIAN, VELKOV, TONY · 2017 to 2021
$4.3M
NIAID NIH HHS R01 AI132154
6 · The paper itself

Abstract

objectivesOptimal dosage regimens of colistin for the treatment of urinary tract infections (UTI) are unknown. Colistimethate sodium (CMS), the inactive prodrug of colistin, is mainly excreted in urine and converts to colistin after filtration by glomeruli, suggesting that concentrations of colistin in urine could be much higher than in plasma. Therefore, there is a need to optimize dosage regimens of intravenous CMS for UTI. The aim of this study was to examine the relationship between AUC/MIC of formed colistin and clinical outcomes in patients with UTI caused by extremely drug resistant (XDR) Pseudomonas aeruginosa.

methodsThis prospective, observational cohort study involved patients with UTI caused by XDR P. aeruginosa. Clinical cure, bacteriological clearance and acute kidney injury (AKI) were analyzed. Steady-state colistin plasma concentrations (C

resultsThirty-three patients were included (24 lower UTI and 9 pyelonephritis). The MIC

conclusionsThe currently recommended dosage regimens of CMS showed high efficacy for the treatment of lower complicated UTI caused by XDR P. aeruginosa in non-critically ill patients and in the case of low MIC values, but also a considerable nephrotoxicity rate. Our data suggest that the use of lower CMS doses for lower UTI should be investigated in future studies to minimize the unnecessary nephrotoxicity.

Indexed as

AgedAnti-Bacterial AgentsColistinDrug Resistance, Multiple, BacterialFemaleHumansKidneyMaleMicrobial Sensitivity TestsMiddle AgedProspective StudiesPseudomonas aeruginosaPseudomonas InfectionsTreatment OutcomeUrinary Tract InfectionsAnti-Bacterial AgentsColistinColistin-associated nephrotoxicityColistin plasma concentrationsUrinary tract infections

Identifiers

PMID31265867
PMCPMC7265153
OpenAlexW2967793847

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.